ENST00000547103.7:c.6265G=
MANE Select
|
ENSP00000447211.2:p.Val2089=
|
|
ENST00000642294.1:c.205G=
|
ENSP00000493572.1:p.Val69=
|
|
ENST00000646859.1:c.6130G=
|
ENSP00000496036.1:p.Val2044=
|
|
ENST00000298820.7:c.1527+123G=
|
|
|
ENST00000458043.6:c.6238G=
|
ENSP00000400895.2:p.Val2080=
|
|
ENST00000546620.5:n.521G=
|
|
|
ENST00000547103.5:c.6202G=
|
ENSP00000447211.1:p.Val2068=
|
|
ENST00000550182.2:c.289G=
|
ENSP00000449641.1:p.Val97=
|
|
ENST00000551340.5:c.393G=
|
|
|
NM_173591.3:c.6238G=
|
NP_775862.3:p.Val2080=
|
|
XM_005268802.2:c.6289G=
|
XP_005268859.1:p.Val2097=
|
|
XM_011538191.1:c.6289G=
|
XP_011536493.1:p.Val2097=
|
|
XM_011538192.1:c.6136G=
|
XP_011536494.1:p.Val2046=
|
|
XM_011538193.1:c.5923G=
|
XP_011536495.1:p.Val1975=
|
|
XM_005268802.3:c.6289G=
|
XP_005268859.1:p.Val2097=
|
|
XM_011538192.2:c.6136G=
|
XP_011536494.1:p.Val2046=
|
|
NM_001368062.1:c.6103G=
|
NP_001354991.1:p.Val2035=
|
|
NM_001368062.3:c.6130G=
|
NP_001354991.2:p.Val2044=
|
|
NM_001378609.3:c.6265G=
MANE Select
|
NP_001365538.2:p.Val2089=
|
|
NM_001378610.3:c.6265G=
|
NP_001365539.2:p.Val2089=
|
|
NM_173591.7:c.6265G=
|
NP_775862.4:p.Val2089=
|
|